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. 2023 Jul;29(7):460.e1-460.e9.
doi: 10.1016/j.jtct.2023.04.011. Epub 2023 Apr 21.

Transplantation Referral Patterns for Patients with Newly Diagnosed Higher-Risk Myelodysplastic Syndromes and Acute Myeloid Leukemia at Academic and Community Sites in the Connect® Myeloid Disease Registry: Potential Barriers to Care

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Transplantation Referral Patterns for Patients with Newly Diagnosed Higher-Risk Myelodysplastic Syndromes and Acute Myeloid Leukemia at Academic and Community Sites in the Connect® Myeloid Disease Registry: Potential Barriers to Care

Benjamin Tomlinson et al. Transplant Cell Ther. 2023 Jul.

Abstract

Hematopoietic stem cell transplantation (HCT) is indicated for patients with higher-risk (HR) myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). Age, performance status, patient frailty, comorbidities, and nonclinical factors (eg, cost, distance to site) are all recognized as important clinical factors that can influence HCT referral patterns and patient outcomes; however, the proportion of eligible patients referred for HCT in routine clinical practice is largely unknown. This study aimed to assess patterns of consideration for HCT among patients with HR-MDS and AML enrolled in the Connect® Myeloid Disease Registry at community/government (CO/GOV)- or academic (AC)-based sites, as well as to identify factors associated with rates of transplantation referral. We assessed patterns of consideration for and completion of HCT in patients with HR-MDS and AML enrolled between December 12, 2013, and March 6, 2020, in the Connect Myeloid Disease Registry at 164 CO/GOV and AC sites. Registry sites recorded whether patients were considered for transplantation at baseline and at each follow-up visit. The following answers were possible: "considered potentially eligible," "not considered potentially eligible," or "not assessed." Sites also recorded whether patients subsequently underwent HCT at each follow-up visit. Rates of consideration for HCT between CO/GOV and AC sites were compared using multivariable logistic regression analysis with covariates for age and comorbidity. Among the 778 patients with HR-MDS or AML enrolled in the Connect Myeloid Disease Registry, patients at CO/GOV sites were less likely to be considered potentially eligible for HCT than patients at AC sites (27.9% versus 43.9%; P < .0001). Multivariable logistic regression analysis with factors for age (<65 versus ≥65 years) and ACE-27 comorbidity grade (<2 versus ≥2) showed that patients at CO/GOV sites were significantly less likely than those at AC sites to be considered potentially eligible for HCT (odds ratio, 1.6, 95% confidence interval, 1.1 to 2.4; P = .0155). Among patients considered eligible for HCT, 45.1% (65 of 144) of those at CO/GOV sites and 35.7% (41 of 115) of those at AC sites underwent transplantation (P = .12). Approximately one-half of all patients at CO/GOV (50.1%) and AC (45.4%) sites were not considered potentially eligible for HCT; the most common reasons were age at CO/GOV sites (71.5%) and comorbidities at AC sites (52.1%). Across all sites, 17.4% of patients were reported as not assessed (and thus not considered) for HCT by their treating physician (20.7% at CO/GOV sites and 10.7% at AC sites; P = .0005). These findings suggest that many patients with HR-MDS and AML who may be candidates for HCT are not receiving assessment or consideration for transplantation in clinical practice. In addition, treatment at CO/GOV sites and age remain significant barriers to ensuring that all potentially eligible patients are assessed for HCT.

Keywords: Acute myeloid leukemia; Bone marrow transplantation; Clinical practice; Hematologic malignancies; Management and treatment; Myelodysplastic syndromes.

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Conflict of interest statement

Conflict of interest statement: B.T. reports serving on a speakers bureau for Bristol Myers Squibb. M.dL. reports current employment at Blood and Bone Marrow Transplant and Cellular Therapy Program, Ohio State University Comprehensive Cancer Center and advisory board membership for Bristol Myers Squibb, Novartis, and Pfizer. C.R.C. has no conflicts of interest to disclose. M.A.T. reports employment at Tempus Labs; advisory board membership/consultancy for AbbVie, Adaptive, Elsevier Clinical Path, Epizyme, GRAIL/Illumina, Janssen, Sanofi, Takeda, and UpToDate; advisory board membership and equity ownership in Doximity; institutional research funding from AbbVie, Amgen, Bristol Myers Squibb, CRAB CTC, Denovo, Glaxo Smith Kline, Hoosier Research Network, Janssen, Lilly, LynxBio, Strata Oncology, Takeda, and TG Therapeutics; royalties from UpToDate; and travel expenses from Syapse Precision Medicine Council. D.L.G. reports advisory board membership for Astellas and advisory board membership/consultancy for Bristol Myers Squibb. D.A.P. reports research funding from AbbVie, Bristol Myers Squibb, and Teva; and advisory board membership/consultancy for AbbVie, Arcellx, AstraZeneca, Bergen Bio, BeiGene, Bristol Myers Squibb, Genentech, Hibercell, Immunogen, Jazz, Kura, Magenta, Medivir, Novartis, Qihan, Ryvu, Syros, and Zentalis. R.S.K. reports consultancy for Agios, Bristol Myers Squibb, Daiichi Sankyo, Incyte, Janssen, and Pfizer; advisory board and speakers bureau membership for Alexion; and speakers bureau membership for Jazz Pharmaceuticals and Novartis. G.J.R. reports consultancy for AbbVie, Amphivena Therapeutics, Argenx, Astex Pharmaceuticals, Bayer, Bristol Myers Squibb, Celltrion, Daiichi Sankyo, Eisai, Janssen, Jazz Pharmaceuticals, Novartis, Orsenix, Otsuka, Pfizer, Roche, and Sandoz; and research funding from Cellectis. M.R.S. reports advisory board membership and consultancy for AbbVie; intellectual property rights and royalties from Boehringer Ingelheim; advisory board membership for Bristol Myers Squibb; research funding from Astex Pharmaceuticals and Incyte; advisory board membership and research funding from Takeda and TG Therapeutics; advisory board membership, consultancy, and equity ownership from Karyopharm Therapeutics; advisory board membership for Ryvu Therapeutics; data and safety monitoring board membership for Sierra Oncology; and research funding from Sunesis Pharmaceuticals. M.A.S. reports advisory board membership for Bristol Myers Squibb, Kurome, and Novartis. M.A. reports advisory board membership for Bristol Myers Squibb and speakers panel membership for AbbVie, Bristol Myers Squibb, Gilead, Seattle Genetrix, and Takeda. G.G-M. has no conflicts of interest to disclose. S.E.K. reports consultancy for Agios, Bristol Myers Squibb, and Incyte. J.P.M. has no conflicts of interest to disclose. J.L.P. reports consultancy for Bristol Myers Squibb. D.A.R. reports consultancy for AbbVie, Allergan, Amgen, Bristol Myers Squibb, Cytokinetics, and Takeda. T.I.G. reports consultancy, scientific steering committee member for Bristol Myers Squibb. E.D.F. reports employment at Bristol Myers Squibb. P.K., I.S.D., and M.N. report employment and equity ownership with Bristol Myers Squibb. C.U.L. reports current employment at CRIPSR Therapeutics and previous employment and equity ownership with Bristol Myers Squibb. H.P.E. reports speakers bureau membership for AbbVie, Bristol Myers Squibb, Incyte, Jazz Pharmaceuticals, Novartis, and Servier; consultancy for AbbVie, Agios, Astellas, Bristol Myers Squibb, Daiichi Sankyo, Glycomimetics, Immunogen, Incyte, Jazz, Kura Oncology, MacroGenics, Novartis, Pfizer, Servier, Syros, Takeda, and Trillium; contracted research for AbbVie, ALX Oncology, Amgen, Ascentage, Daiichi Sankyo, Forma, Gilead, Glycomimetics, Immunogen, Jazz Pharmaceuticals, MacroGenics, Novartis, PTC, and Sumitomo Pharma; independent review committee chair for AbbVie; and steering committee membership for Bristol Myers Squibb and Glycomimetics. D.P.S. reports employment at Novartis and minor equity in bluebird bio and Gamida Cell. B.L.S. reports speakers bureau membership for Agios; advisory board and speakers bureau membership and consultancy for Alexion and Bristol Myers Squibb; advisory board and speakers bureau membership for Incyte; and research funding from Novartis.

Figures

Figure 1.
Figure 1.
Reasons cited for being considered not eligible for transplantation in patients from the total study population (A) and those considered potentially eligible candidates (B). Multiple answers per patient are possible.

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